US3549317A - Process for utilizing fluorosilicic acid - Google Patents

Process for utilizing fluorosilicic acid Download PDF

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US3549317A
US3549317A US745621A US3549317DA US3549317A US 3549317 A US3549317 A US 3549317A US 745621 A US745621 A US 745621A US 3549317D A US3549317D A US 3549317DA US 3549317 A US3549317 A US 3549317A
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sif
acid
solution
silica
sio
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Ludwig Dorn
Ernst Podschus
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Bayer AG
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    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00—Silicon; Compounds thereof
    • C01B33/113—Silicon oxides; Hydrates thereof
    • C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
    • C01B33/187—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by acidic treatment of silicates
    • C01B33/193—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by acidic treatment of silicates of aqueous solutions of silicates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/10—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate
    • B01J20/103—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate comprising silica
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00—Silicon; Compounds thereof
    • C01B33/113—Silicon oxides; Hydrates thereof
    • C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
    • C01B33/186—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof from or via fluosilicic acid or salts thereof by a wet process
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F11/00—Compounds of calcium, strontium, or barium
    • C01F11/20—Halides
    • C01F11/22—Fluorides
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/12—Surface area

Definitions

  • a silica filler e.g. having a specific surface area of between about 50-200 m. /g., and calcium fluoride by the steps of (a) reacting fluorosilicic acid (H SiF and/or sodium fluorosilicate (Na SiF with a concentration of e.g. 1040% by weight in aqueous medium with calcium carbonate having a concentration of at least about 100 g.
  • step (c) precipitating the silica filler from said silicate solution from step (b) at a temperature above about 50 C., by gradual, dilution with a mineral acid to neutralize said solution to a pH value of between about preferably, with optimal use of fluorosilicic acid in a form prepared by prior introduction of SiF into water or dilute fluorosilicic acid to hydrolyze the SiF, until a concentration therein of at least 10% by weight H SiF is obtained, and with optional recovery and washing of the silica precipitate resulting from such hydrolysis, fol- Y lowed by dissolving thereof in sodium hydroxide solution .at a SiO /NaOH ratio of more than about 1:05 and combining of the resulting solution with the silicate solution from step (h) prior to dilution with acid in step (c).
  • the present invention relates to a process for exploiting fluorosilicic acid.
  • the SiF, formed in the production of hydrofluoric acid and phosphates is usually converted into fluorosilicic acid and fluorosilicates.
  • numerous processes have already been proposed for producing hydrofluoric acid or fluorides and silica from SiF, and silicofluorides.
  • SiF is introduced into Water, yielding silica and fluorosilicic acid which, after removal of the silica, is then reacted with CaCO to give Caland silicic acid. After filtration and drying, the resulting mixture is reacted with sulfuric acid to give, besides C3804 and HF, also SiF which is again introduced into water and the process repeated.
  • the silica obtained from the hydrolysis of SiF is intended to be used as a filler. Unfortunately, the silica obtained in this way is not competitive in its properties with the silica fillers that are currently available on the market, particularly in their capacity as fillers for reinforcing rubbers.
  • Fluorosilicic acid or sodium fluorosilicate is reacted with calcium carbonate at a temperature of at least 50 C. and with a concentration of at least g. of CaCO /l. in a molar ratio of about 1:3 or 1:2, respectively;
  • reaction mixture is reacted while still hot with at least 10% sodium hydroxide in a quantity of from 1 to 3 mols of NaOH per mol of SiO and the resulting silicate solution is separated from the CaF deposit;
  • a silicate filler is precipitated from the silicate solution at a temperature above 50 C. by the gradual addition of acid up to a pH value of from 7 to 9.
  • the starting material for the production of fluorosilicic acid which is generally handled in the form of a 20 to 30% solution, is SiF which is formed from the silica present in fluorspar or apatite.
  • SiF silicic acid and fluorosilicic acid are formed in accordance with the equation:
  • silica formed during this reaction can be filtered fairly readily in the presence of fairly high concentrations of H SiF As already mentioned, however, it is not suitable for use in the reinforcing of rubbers or as a paper filler.
  • fluorosilicic acid and/or of sodium silicofluoride in accordance with the invention, it has proved to be of advantage to dissolve the silica obtained from SiF, in the preceding hydrolysis stage under the effect of heat in at least 5%, and preferably from 5 or 7 to 15%, sodium hydroxide solution in a ratio of SiO /NaO H of more than about 1:05 e.g.
  • fluorosilicic acid preferably in the form of an approximately 10 to 40% solution
  • CaCO preferably in a concentration of from about 100' or 200 to 300 g./l., advantageously in the form of powdered calcite, at a temperature of about 50 C. and preferably at a temperature of from about 50 or 60 C. to the boiling temperature.
  • the end of the reaction is clearly recognizable from the cessation of the Co -evolution.
  • the reaction can be carried out either continuously or in batches. In cases where the reaction is carried out in batches, the order in which the additions are made is not important. However, it is preferred initially. to introduce the CaCO suspension for reasons of minimizing corrosion.
  • the calcium. fluoride which contains approximately 50% or less of water, is dried, optionally ground and then reacted in known manner with concentrated sulfuric acid, for example, by the method used to produce hydrofluoric acid, i.e. to form CaSO and HF.
  • an acid preferably fluorosilicic acid or other mineral acids such as sulfuric acid, and optionally at least to some extent CO in order to precipitate silica with the properties of a filler.
  • the acid is gradually added with stirring at a substantially uniform rate over a period ranging from some 10 minutes up to 2 hours, addition of the acid being terminated after a pH-value of between about 7 and 9 has been reached.
  • the suspension is then maintained for 10 to 180 minutes to a temperature of at least about 90- C. up to the boiling temperature and subsequently filtered.
  • the silica is washed, driedpreferably by spray-drying-and ground.
  • the washing stage is with advantage followed by neutralization with a mineral acid, e.g. sulfuric acid so as i to adjust to a weakly acid pH value of about to 6.5, followed again by washing.
  • the filterability of the calcium fluoride left after the second stage of the process from the silicate solution can be improved by the addition of known flocculating agents, such as, for example, cation-active flocculating agents, for example, polyamines.
  • flocculating agents such as, for example, cation-active flocculating agents, for example, polyamines.
  • the filterability of the calcium fluoride formed from sodium silico-fluoride and .separated from an NaF-containing sodium'silicate solution is better from the outset so that there is no need in this case toadd flocculating agents.
  • a small amount of NaF is also present in the silicate solution formed from H SiF because the reaction does not proceed strictly in accordance with Equation 11 given hereinabove.
  • a little silicic acid is always left behind in, the calcium fluoride, and a little NaF in the silcate soluton. to of the Si present in the fluorosilicic acid or in the fluorosilicate is separated in the form of a silicate solution however.
  • the process according to the invention is also suitable for working up sodium silicofluoride, even contaminated material of the kind precipitated as a secondary product in the wet process for the production of phosphoric acid, in conjunction with the production of hydrofluoric acid from fluorspar and sulphuric acid.
  • the resulting calcium fluoride which contains the impurities such as,
  • solubility of NaF amounts only to about 1 mol per litre, it is of advantage to adjust the reaction concentration and the quantity of washing water used in such a way that, during filtration of the CaF the filtrate and the washing water accumulate in such quantities that the NaF formed in the first stage and the NaF formed during subsequent precipitation of the filler can still just be dissolved, i.e. the quantity of water used during the reaction, based on 1 mol of Na siFg, is just suflicient to enable the reaction mixture to be readily stirred, the CaF filtered off being washed until the required volume has been obtained.
  • filtrate and washing water should together make up approximately 3 liters per mol of Na SiF used so that the quantity of NaF formed initially remains in solution with the sodium silicate.
  • the NaF aformed also remains in solution during the subsequent precipitation of the silica filler.
  • the dilute and at most approximately '1 molar NaF solutions formed during the working up of the silicate solution into silicate fillers may be used in the production of cryolite, or alternatively may even be converted into CaF by reaction with lime while any CaF may be treated with mineral acid to produce hydrofluoric acid in the conventional manner.
  • H SiF solution flowing in through a line b is reacted in an agitation tank A with a CaCO suspension which has already been run into the tank A from a line a.
  • the reaction mixture is transferred from the tank A into a tank B containing sodium hydroxide which was fed in via line c.
  • the CaF is separated and washed in a suction filter C, and the resulting filtrate is treated with acid in a tank D in order to precipitate the SiO filler.
  • the CO removed from the tank A through a line d may be used for this purpose, in which case filtration in filter C need only be followed by the addition of acid through the line f in the quantities suflicient to adjust a weakly acid pH value.
  • the resulting SiO precipitate is separated in a separator E.
  • the NaF-containing solution run oif through the line 2 may be used, forexample, for the production of cryolite.
  • the process described above may be combined with the production of HgSiFs from SiF in which case v.SiE, is reacted with water in a tank F.
  • the reaction mixture is separated from Si0 in a separator G.
  • a tank H the SiO is dissolved in sodium hydroxide solution from a line c and the resulting solution is transferred to the tank D, whilst the H SiF solution flows from the tank F through the line b into the tank A where it is reacted.
  • EXAMPLE 1 400 g. (4 mols) of powdered calcite (CaCO were suspended in 2 litres of water in a S-litre-capacity vessel, and the resulting suspension was heated to 95 C. 376 g. (2 mols) of powdered sodium fluorosilicate (Na- SiF were then added in portions to the suspension over a period of 30 minutes. The reaction was accompanied by the vigorous evolution of CO gas. The reaction mixture was stirred for another 60 minutes at 95 C., and slowly poured with stirring over a period of 5 minutes into 750 ml. of hot, 4-molar sodium hydroxide. The suspension was stirred for another 90 minutes at 95 C., and filtered olf through a pre-heated suction filter.
  • powdered calcite CaCO
  • the filter cake (530 g.) was dried at 120 C. 306 g. of powdered product were obtained. It consisted of 296 g. (approx. 3.8 mols) of CaF 86 g. of SiO 0.9 g. of CaO and 0.5 g. of Na O. This corresponds to a proportion by weight of 2.8% of SiO in the calcium fluoride. Based on the quantity of SiO used in the form of Na SiF approx tely 6% was left undissolved in the solid.
  • the filtrate was then combined with intensive stirring over a period of minutes at 60 C. with 140 ml. of a 2.8 molar H SiF solution that was uniformly run in.
  • the pH value of the reaction mixture dropped to 8.5. This was followed by some thirty minutes heating to boiling point, after which the silica precipitated was filtered off, washed, adjusted to pH 6 with dilute sulfuric acid, dried at 110 C. and ground.
  • the filler thus obtained was eminently suitable for reinforcing rubbers.
  • the filtrate (6.4 1.) contained 40 g. of NaF and 0.5 g. of SiO per litre.
  • EXAMPLE 2 30 kg. (300 mols) of calcite were suspended in 100 1. of water in a 200 litre-capacity vessel equipped with a propellor agitator and the resulting suspension was heated to between 90 and 95 C. 35.8 litres of a 2.8 molar aqueous H SiF solution were then-added over a period of 100 minutes. The reaction is characterized by the vigorous evolution of C0 The reaction mixture was then heated with stirring for another 30 minutes to between 95 and 100 C., the suspension was introduced with stirring over a period of 30 minutes into 25 litres of a 19.6% hot sodium hydroxide solution (approximately 150 mols of NaOH), followed by another 15 minutes stirring at 95 C. 36 g. of a cation-active-polyamine fiocculating agent were added to the hot suspension which was then filtered on a filter press and washed.
  • a cation-active-polyamine fiocculating agent were added to the hot suspension which was then filtered on a filter
  • the filter cake which contained approximately 45% of water was dried at 120 C. 24 kg. of calcium fluoride containing 36% of Si0 and 115 litres of filtrate containing 0.85 mol of (Na O) .SiO and approximately 7 g. of NaF per litre were obtained.
  • a silica filler with a specific surface of 100 m. g. according to BET was obtained from this solution over a period of 45 minutes by the uniform addition thereto with intensive stirring of 3-normal sulfuric acid at 60 C. followed by drying.
  • Process for the production of a silica filler and calcium fiuoride which comprises (a) reacting a member selected from the group consisting of fluorosilicic acid, sodium fiuorosilicate, and
  • step (b) reacting the resulting still hot CaF and SiO -containing reaction mixture from step (a) with at least about 10% sodium hydroxide in an amount of between about 1-3 mols of NaOH per mol of SiO present and separating the resulting silicate solution from the CaF precipitate, and
  • step (c) precipitating the silica filler from said silicate solution from step (b) at a temperature above about 50 C. by the gradual dilution with acid to neutralize said solution to a pH value of between about 7-9, whereby to produce a silica filler having a specific surface area between 50-200 m. g.
  • step (a) wherein said member is reacted in step (a) at a concentration in water ofbetween about 10-40% by weight with calcium carbonate having a concentration in water of between about 100 300 g./liter, at a temperature between about 50 C. and the boiling temperature.
  • said member is fluorosilicic acid which is used in a form prepared by the prior introduction of SiF into a hydrolysis medium selected from the group consisting of water and dilute fluorosilicic acid for corresponding hydrolysis of such SiF in said medium until a concentration therein of at least 10% by weight HgSlFs is obtained and wherein the silica precipitate correspondingly formed during such hydrolysis is washed, then dissolved in sodium hydroxide solution at a SiO /NaOH ratio of more than about 1:05 and thereafter combined with the silicate solution from step (b) prior to dilution with acid in step (c).
  • a hydrolysis medium selected from the group consisting of water and dilute fluorosilicic acid for corresponding hydrolysis of such SiF in said medium until a concentration therein of at least 10% by weight HgSlFs is obtained and wherein the silica precipitate correspondingly formed during such hydrolysis is washed, then dissolved in sodium hydroxide solution at a SiO /NaOH ratio of more
  • Process according to claim 1 for the production of a silica filler and calcium fluoride which comprises (a) reacting in water a member selected from the group consisting of H SiF Na SiF and mixtures thereof, at a concentration of between about 10-40% by weight, with CaCO at a concentration of between about 100-300 g./ liter, and in a corresponding molar ratio of said member to CaCO of between about 1:3 to 1:2, at a temperature between about 50 C.
  • step (b) reacting the resulting still hot reaction mixture from step (a) with NaOH solution having a concentration of between about 10-50% by weight NaOH 7 and in an amount of between about 1-3 mols of References Cited NaOHrper mol of SiO present and separating the resulting silicate solution from the CaF precipitate, UNITED S'FQATES PATENTS and 1,382,165 6/1921 Bishop 23-110x
  • step (c) preparing the silica filler from said silicate solution 1,634,122 6/1927 Stevmson 23 110X from step (b) by precipitating, removing said pre- 2,561,304 7/1951 Haze ⁇ 23182 cipitate from the reaction medium, washing, drying 2,588,853 3/1952 Kumms et 23182 and grinding, wherein the precipitation is effected by 2,601,235 6/1952 Alexander et 23-182 gradually neutralizing said silicate solution 'with an 2,780,521 2/1957 Butt 23

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  • Silicon Compounds (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
US745621A 1967-08-12 1968-07-17 Process for utilizing fluorosilicic acid Expired - Lifetime US3549317A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4213952A (en) * 1978-10-23 1980-07-22 Occidental Research Corporation Recovery of hydrofluoric acid from fluosilicic acid with high pH hydrolysis
US4213951A (en) * 1978-10-23 1980-07-22 Occidental Research Corporation Recovery of hydrofluoric acid from fluosilicic acid with high pH hydrolysis
US4298586A (en) * 1978-10-23 1981-11-03 Occidental Research Corp. Recovery of hydrofluoric acid from fluosilicic acid
US4308244A (en) * 1980-03-28 1981-12-29 Occidental Research Corp. Process for producing fluorine compounds and amorphous silica
US4915705A (en) * 1986-08-01 1990-04-10 Freeport Research And Engineering Co. Production of silica and fluorine-containing coproducts from fluosilicic acid
US5910297A (en) * 1997-07-31 1999-06-08 E. I. Du Pont De Nemours And Company Alkaline earth fluoride manufacturing process
US20160108244A1 (en) * 2013-05-16 2016-04-21 Thomas E Kane Silica protected pigments for use in artist media
CN115192465A (zh) * 2021-04-08 2022-10-18 北京化工大学 CaF2@SiO2纳米颗粒或团簇体的制备方法

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2307897C3 (de) * 1973-02-17 1982-02-18 Bayer Ag, 5090 Leverkusen Verfahren zur Herstellung von synthetischem Flußspat
US4078043A (en) * 1974-02-15 1978-03-07 Kali-Chemie Aktiengesellschaft Process for preparing calcium fluoride from hexafluoro silicic acid and production of silicic acid gel or active silicic acid from said calcium fluoride
AT375627B (de) * 1980-04-30 1984-08-27 Voest Alpine Ag Verfahren zur aufarbeitung von beim nassaufschluss von phosphaten anfallender kieselfluorwasserstoffsaeure sowie einrichtung zur durchfuehrung des verfahrens
WO2021079368A1 (en) 2019-10-24 2021-04-29 IMI Tami Institute for Research and Development ltd Novel flux / mineralizer for cement clinkering and method of manufacture thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1382165A (en) * 1919-08-30 1921-06-21 Howard B Bishop Process of making fluorids
US1634122A (en) * 1921-10-08 1927-06-28 Little Inc A Method of producing sodium fluoride
US2561304A (en) * 1947-10-30 1951-07-17 Philadelphia Quartz Co Process for the production of finely divided amorphous silica
US2588853A (en) * 1948-07-02 1952-03-11 Interchem Corp Method of producing silica powder
US2601235A (en) * 1949-06-15 1952-06-24 Du Pont Process for producing built-up silica particles
US2780521A (en) * 1954-03-22 1957-02-05 Int Minerals & Chem Corp Process for producing colloidal silicafree calcium fluoride
US2780523A (en) * 1954-03-22 1957-02-05 Int Minerals & Chem Corp Process for recovering solid calcium fluoride containing product and colloidal silica solution from a weak aqueous fluosilicic acid solution
US2881049A (en) * 1954-09-28 1959-04-07 Hoechst Ag Process of preparing alkali metal silicates
US3445189A (en) * 1965-03-05 1969-05-20 Koninkl Zwavelzuurfabrieken V Process for the production of a finely divided,non-gelatinous silicic acid especially suitable as a filler for natural and synthetic rubber and other elastomers

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1382165A (en) * 1919-08-30 1921-06-21 Howard B Bishop Process of making fluorids
US1634122A (en) * 1921-10-08 1927-06-28 Little Inc A Method of producing sodium fluoride
US2561304A (en) * 1947-10-30 1951-07-17 Philadelphia Quartz Co Process for the production of finely divided amorphous silica
US2588853A (en) * 1948-07-02 1952-03-11 Interchem Corp Method of producing silica powder
US2601235A (en) * 1949-06-15 1952-06-24 Du Pont Process for producing built-up silica particles
US2780521A (en) * 1954-03-22 1957-02-05 Int Minerals & Chem Corp Process for producing colloidal silicafree calcium fluoride
US2780523A (en) * 1954-03-22 1957-02-05 Int Minerals & Chem Corp Process for recovering solid calcium fluoride containing product and colloidal silica solution from a weak aqueous fluosilicic acid solution
US2881049A (en) * 1954-09-28 1959-04-07 Hoechst Ag Process of preparing alkali metal silicates
US3445189A (en) * 1965-03-05 1969-05-20 Koninkl Zwavelzuurfabrieken V Process for the production of a finely divided,non-gelatinous silicic acid especially suitable as a filler for natural and synthetic rubber and other elastomers

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4213952A (en) * 1978-10-23 1980-07-22 Occidental Research Corporation Recovery of hydrofluoric acid from fluosilicic acid with high pH hydrolysis
US4213951A (en) * 1978-10-23 1980-07-22 Occidental Research Corporation Recovery of hydrofluoric acid from fluosilicic acid with high pH hydrolysis
US4298586A (en) * 1978-10-23 1981-11-03 Occidental Research Corp. Recovery of hydrofluoric acid from fluosilicic acid
US4308244A (en) * 1980-03-28 1981-12-29 Occidental Research Corp. Process for producing fluorine compounds and amorphous silica
US4915705A (en) * 1986-08-01 1990-04-10 Freeport Research And Engineering Co. Production of silica and fluorine-containing coproducts from fluosilicic acid
US5910297A (en) * 1997-07-31 1999-06-08 E. I. Du Pont De Nemours And Company Alkaline earth fluoride manufacturing process
US20160108244A1 (en) * 2013-05-16 2016-04-21 Thomas E Kane Silica protected pigments for use in artist media
US9994714B2 (en) * 2013-05-16 2018-06-12 Thomas E. Kane Silica protected pigments for use in artist media
CN115192465A (zh) * 2021-04-08 2022-10-18 北京化工大学 CaF2@SiO2纳米颗粒或团簇体的制备方法

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GB1239078A (es) 1971-07-14
NL6811308A (es) 1969-02-14
DE1667500A1 (de) 1971-06-16
FR1580578A (es) 1969-09-05
AT286930B (de) 1970-12-28

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